1973
DOI: 10.1126/science.179.4073.588
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Selenium: Biochemical Role as a Component of Glutathione Peroxidase

Abstract: When hemolyzates from erythrocytes of selenium-deficient rats were incubated in vitro in the presence of ascorbate or H(2)O(2), added glutathione failed to protect the hemoglobin from oxidative damage. This occurred because the erythrocytes were practically devoid of glutathione-peroxidase activity. Extensively purified preparations of glutathione peroxidase contained a large part of the (75)Se of erythrocytes labeled in vivo. Many of the nutritional effects of selenium can be explained by its role in glutathi… Show more

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Cited by 6,752 publications
(2,992 citation statements)
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“…In the early part of the 1970s, a specific biological role for Se became apparent with the discovery of the first selenoprotein glutathione peroxidase (GSH-Px; Rotruck et al, 1973). GSH-Px catalyses the reduction of lipid and hydrogen peroxides to less harmful hydroxides via the oxidation and subsequent reduction of the selenocysteine (SeCys) active centre of the enzyme (Surai, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…In the early part of the 1970s, a specific biological role for Se became apparent with the discovery of the first selenoprotein glutathione peroxidase (GSH-Px; Rotruck et al, 1973). GSH-Px catalyses the reduction of lipid and hydrogen peroxides to less harmful hydroxides via the oxidation and subsequent reduction of the selenocysteine (SeCys) active centre of the enzyme (Surai, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…Total SOD activity was assayed by measuring the absorbance at 560 nm (Ljutakova, 1984). GSH-Px activity was assessed by the method based on the reaction between the GSH which remained after the action of GSH-Px and 5,5 0 -dithiobis-2-nitrobenzoic acid to form a complex with maximal absorbance at 412 nm (Rotruck et al, 1973). Lipid peroxidation was calculated by MDA production as measured by the spectrophotometric color produced during the reaction of the thiobarbituric acid with MDA at 532 nm (Agostinho et al, 1997).…”
Section: Biochemical Determinationsmentioning
confidence: 99%
“…Catalase (CAT) activity was measured by following decomposition of H202 according to the method of Berr's and Sizer (17). Glutathione pemxidase (GSH-Px) was assayed by the method of Rotruck et al (18) using H202 as substrate.…”
Section: Indian Journal Of Clinica/ Biochemistry 2004mentioning
confidence: 99%